US8945497B2 - Catalyst and process - Google Patents

Catalyst and process Download PDF

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US8945497B2
US8945497B2 US13/119,605 US200913119605A US8945497B2 US 8945497 B2 US8945497 B2 US 8945497B2 US 200913119605 A US200913119605 A US 200913119605A US 8945497 B2 US8945497 B2 US 8945497B2
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catalyst
weight
oxidation
gas stream
ruthenium
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US20110229396A1 (en
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Gareth Headdock
Kenneth George Griffin
Peter Johnston
Martin John Hayes
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Johnson Matthey PLC
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/56—Platinum group metals
    • B01J23/64—Platinum group metals with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/656—Manganese, technetium or rhenium
    • B01J23/6562—Manganese
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
    • B01J23/46—Ruthenium, rhodium, osmium or iridium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34—Chemical or biological purification of waste gases
    • B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
    • B01D53/86—Catalytic processes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
    • B01J23/46—Ruthenium, rhodium, osmium or iridium
    • B01J23/462—Ruthenium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/56—Platinum group metals
    • B01J23/63—Platinum group metals with rare earths or actinides
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/56—Platinum group metals
    • B01J23/64—Platinum group metals with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/656—Manganese, technetium or rhenium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/89—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/89—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals
    • B01J23/8913—Cobalt and noble metals
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2251/00—Reactants
    • B01D2251/10—Oxidants
    • B01D2251/102—Oxygen
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2255/00—Catalysts
    • B01D2255/10—Noble metals or compounds thereof
    • B01D2255/102—Platinum group metals
    • B01D2255/1026—Ruthenium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2255/00—Catalysts
    • B01D2255/20—Metals or compounds thereof
    • B01D2255/207—Transition metals
    • B01D2255/2073—Manganese
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2255/00—Catalysts
    • B01D2255/20—Metals or compounds thereof
    • B01D2255/207—Transition metals
    • B01D2255/20746—Cobalt
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2257/00—Components to be removed
    • B01D2257/70—Organic compounds not provided for in groups B01D2257/00 - B01D2257/602
    • B01D2257/702—Hydrocarbons
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2257/00—Components to be removed
    • B01D2257/70—Organic compounds not provided for in groups B01D2257/00 - B01D2257/602
    • B01D2257/708—Volatile organic compounds V.O.C.'s
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
    • B01J21/04—Alumina
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals

Definitions

  • the present invention concerns the removal of volatile organic compounds (VOCs) from gas streams.
  • VOCs volatile organic compounds
  • the invention is useful for the purification of inert gas streams containing organic materials such as hydrocarbons and glycols which are present in the gas stream exiting a solid phase polymerisation (SPP) process, although the process and catalyst are not limited to the use in that application.
  • SPP solid phase polymerisation
  • the oxidation catalyst used in the purification process is typically either platinum (Pt) or palladium (Pd) or a mixture of them, supported on a solid support material such as alumina.
  • EP-A-0660746 describes a process for the purification of inert gas stream containing organic impurities from an SPP reactor comprising adding oxygen or gas containing oxygen to the gas stream and circulating the gas stream through a catalytic bed containing Pt or mixtures of Pt and Pd supported on an inert porous support at temperatures from 250 to 600° C. The process is characterized in that the quantity of oxygen used is stoichiometric with respect to the organic impurities or in such an excess that the gas at the outlet of the oxidation reactor contains up to 10 ppm of oxygen.
  • the process for the oxidation of organic compounds may be improved by the use of a novel catalyst not disclosed in the prior art.
  • the present invention provides an improved process for the oxidation of organic compounds in a gas stream.
  • the invention further provides a novel catalyst which is useful for the oxidation of organic compounds in a gas stream.
  • a process for the oxidation of organic compounds contained in a gas stream comprises the step of introducing said gas stream containing the organic compounds into a reactor containing an oxidation catalyst together with sufficient oxygen to effect the desired amount of oxidation and maintaining the temperature of said gas stream at a temperature sufficient to effect oxidation, characterised in that the oxidation catalyst contains at least 0.01% by weight of a metal selected from ruthenium, cobalt or manganese or a combination thereof.
  • the preferred metal is ruthenium.
  • a catalyst comprising a support material, from 0.05-5% by weight of platinum, palladium or a mixture of platinum and palladium; and from 0.01 to 5% by weight, based on the total weight of catalyst metals plus support, of a metal selected from ruthenium, cobalt or manganese or a combination thereof.
  • the preferred metal is ruthenium.
  • FIG. 1 is the percent (%) conversion of ethylene glycol vs. temperature for the catalysts of Examples 1-4 and Comparative Examples 1 and 2;
  • FIG. 2 is the percent (%) conversion of ethylene glycol vs. time for the catalysts of Examples 2 and 9.
  • a catalyst containing ruthenium, cobalt or manganese enables the oxidation process to be carried out at a lower temperature than is typical using a conventional platinum and/or palladium catalyst.
  • the reduction in oxidation temperature has clear economic advantages because the process then requires less energy to operate. For example, in a solid phase polymerisation process, which is typically operated at a temperature of between 210 and 215° C., the gas stream exiting the SPP reactor must be heated up to the operating temperature of the oxidation step and then cooled down before it re-enters the SPP process.
  • the amount of cooling required is less if the oxidation process is run at a lower temperature.
  • the operating temperature of the oxidation is 300° C. as described in the Example of EP-A-660746, then the amount of energy required for heating and cooling the circulating gas stream between 215 and 300° C. may be considerable.
  • the catalyst preferably comprises ruthenium, cobalt or manganese or a compound of ruthenium, cobalt or manganese supported on a solid catalyst support.
  • the catalyst support material is selected from any known support which is stable under the operating conditions of the oxidation reaction.
  • Preferred support materials include alumina (in all forms, including alpha alumina and transition aluminas such as gamma. theta and delta alumina for example), silica, silica-alumina, ceria, titania, zirconia or mixtures of these.
  • a preferred support contains alumina, particularly transition aluminas.
  • Particularly preferred supports include alumina and mixtures of alumina with ceria, especially alumina mixed with up to about 20% by weight of ceria.
  • the support material does not comprise carbon in order to avoid the risk of oxidation of the carbon in the reactor.
  • the support may be modified, treated or coated.
  • an alumina support may be impregnated with a solution of a metal salt such as cerium nitrate which, upon calcination, modifies the support by forming ceria in or on a part of the alumina.
  • the support is preferably porous, most preferably having a porosity greater than 0.3 ml/g, especially >0.5 ml/g.
  • a high surface area support is preferred, for example a support having a surface area >50 m 2 /g, especially >80 m 2 /g is particularly suitable.
  • the physical form of the catalyst may be particulate or massive.
  • Particulate forms include powders, granules, spherical particles, tablets, lobed shaped particles or other 3-dimensional shapes.
  • Typical particles for use in forming fixed catalyst beds for gaseous reactants have a minimum dimension in the range from 1-10 mm.
  • the skilled person will appreciate that the size and shape of the particles affects the flow of gas through the bed and so the appropriate particle dimension may be selected dependent on the amount of gas to be treated and the acceptable pressure drop through the reactor.
  • Powders or granules of a size less than 1 mm, especially from 50-500 ⁇ m may be used if the oxidation reaction is to be carried out in a fluidised bed reactor.
  • Massive forms of catalyst include structured reactors such as catalytic monolith reactors or catalyst materials supported on mesh or foamed supports.
  • the catalyst contains at least 0.01% by weight of ruthenium, cobalt or manganese.
  • the catalyst also contains at least one further metal or metal compound which is preferably a noble metal, more preferably platinum, palladium or a mixture of these.
  • the catalyst comprises a support material, from 0.05 to 5% by weight of platinum, palladium or a mixture of platinum and palladium; and from 0.01 to 5% by weight of ruthenium. More preferably the catalyst comprises from 0.03 to 1% by weight of ruthenium, especially from 0.03 to 0.2% by weight of ruthenium and we have found that a catalyst containing not more than about 0.1% by weight of ruthenium is effective.
  • the content of platinum, palladium or their mixture in the catalyst is preferably from 0.05-2% by weight, more preferably from 0.1 to 1.0% by weight.
  • the catalyst may be promoted with up to 20% by weight of cerium or a compound of cerium, more preferably from 0.1-15% by weight, especially from 2-10% by weight of cerium or a compound of cerium.
  • cerium acts as an effective oxygen management promoter under oxygen lean conditions. All percentages are given by weight based on the total weight of catalyst metals plus support.
  • the catalyst metals i.e. the ruthenium, cobalt and/or manganese and other metals and cerium promoter, if present, may be present as elemental metals or as metal compounds. It is believed that the active form of the metals is the elemental form although other metal compounds may be present.
  • the catalysts are made typically by depositing a compound of the metal in or on a support material followed by a step of reducing the metal compound to the elemental form to produce very fine metal particles on the support.
  • the metal salt may comprise a salt such as a nitrate, chloride, sulphate, carboxylate (e.g.
  • an organic compound such as a ⁇ -diketone or an ammine complex, including an ionic ammine complex such as an ammine chloride for example.
  • the metal compound deposited on the support may be transformed to a different compound by an intermediate step such as calcination as is well-known in the art of catalyst manufacture, but such a step may be unnecessary.
  • the metal compound and/or promoter and/or an intermediate of any of them if present is typically reduced to metallic form by known methods.
  • the reduction step may be performed in the oxidation reactor itself or the catalyst may be reduced ex-situ and transported in reduced form.
  • the reduction is carried out in a stream of a hydrogen-containing gas, which may be pure hydrogen or a mixture of hydrogen and an inert gas, at elevated temperature however alternative reduction methods such as the use of liquid reducing agents, for example hydrazine, formaldehyde, sodium borohydride or an alcohol, may also be used.
  • a catalyst support is impregnated with a solution of the metal salts, e.g.
  • the catalyst is likely to include an oxide of the ruthenium and other metals if present.
  • the process of the invention is preferably a non-selective oxidation in which the objective is to oxidise the organic compounds in the gas stream to carbon dioxide and water.
  • Such a process may be distinguished from a selective oxidation process in which the objective is to oxidise only selected organic compounds in the gas stream or to avoid over-oxidation.
  • the step of purifying the flowing inert gas stream in a solid phase polymerisation (SPP) process typically involves passing the gas stream over an oxidation catalyst, together with sufficient oxygen to oxidise the organic materials to carbon dioxide and water, which are then removed from the gas stream.
  • the temperature of the oxidation process varies from 150° C. to 600° C. depending on the gas stream and application. It is surprising that we have found that the temperature of operation of a purification step in a SPP process may be carried out at a temperature below 250° C., since it is clear that prior art processes using palladium or platinum catalysts specify an operating temperature above 250° C.
  • a process for purifying a gas stream originating from a solid-phase polymerisation reactor, said gas stream comprising an inert gas and a minor amount of one or more organic compounds comprising the step of passing said gas stream together with oxygen over a catalyst, characterised in that the gas stream contacts the catalyst at a temperature of less than 250° C.
  • the contact temperature is between 150 and 249° C., more preferably from 180 to 240° C.
  • the process is operated at a GHSV in the range from 2,000-20,000, especially between 5,000 and 15,000.
  • the inert gas is typically nitrogen.
  • the organic compounds in the gas stream typically include acetaldehyde, an alkylene glycol which is typically ethylene glycol and/or polyester oligomers, hydrocarbons and oxygenated hydrocarbons.
  • the catalyst preferably comprises at least 0.01% of ruthenium, a catalyst support and optionally other metals as described above.
  • the catalyst is particularly suitable for the purification of a gas stream from a solid phase polymerisation reactor, its use in other applications is also contemplated.
  • the catalyst is useful for the catalytic oxidation of volatile organic compounds in a number of industrial applications. Examples include but are not limited to cryogenic gas handling and treatment operations, for example in the purification of gas for supply in bottled form; the destruction of solvent vapours emanating from coating and printing operations; refinery processes, oil and gas treatment and drilling, chemical processes including polymerisation processes, water treatment, processing of natural products such as foods, e.g. roasting, amongst others. In many of these applications, there is no strict limit on the amount of oxygen used and so the process may be operated in the presence of an excess of oxygen.
  • gamma alumina spheres (3 mm diameter, 115 m 2 /g surface area, pore volume 80 ml/100 g) were charged to a laboratory tumbling apparatus and tumbled slowly at about 2 rpm. The mixed solution was added slowly to the tumbling alumina pellets in aliquots over about 10 minutes. The tumbling was continued for a further 15 minutes, and then the catalyst was dried overnight in an air oven at 105° C. The dried catalyst was then transferred to a reduction apparatus and heated to 250° C. in flowing hydrogen. The flow was maintained at this temperature for 2 hours at 250° C. after which the apparatus and catalyst was cooled. The dry catalyst contained 0.15% by weight Pd and 0.14% by weight Ru.
  • Example 1 The method of Example 1 was repeated using as a first solution a solution of 2 g of a solution of platinum nitrate (Pt(NO 3 ) 4 ) in nitric acid containing 15.69% by weight of Pt, made up to 60 ml in demineralised water.
  • the second solution contained 1.1 g of the ruthenium nitrosylnitrate solution made up to 60 ml in demineralised water.
  • the resulting dry catalyst contained 0.15% by weight Pt and 0.08% by weight Ru.
  • Example 2 2.00 g of the platinum nitrate solution used in Example 2 was diluted in 60 ml of demineralised water to form a first solution.
  • a second solution was prepared containing 1% of manganese by weight by dissolving manganese nitrate Mn(NO 3 ) 2 ⁇ 4H 2 O in demineralised water. 4.41 g of the second solution was mixed with the first solution and made up to 150 ml with demineralised water.
  • 208 g of 3 mm alumina spheres as used above were charged to a laboratory tumbling apparatus and tumbled slowly at about 2 rpm. The mixed solution was added slowly to the tumbling alumina pellets in aliquots over about 10 minutes.
  • the tumbling was continued for a further 15 minutes, and then the catalyst was dried overnight in an air oven at 105° C.
  • the dried catalyst was then transferred to a reduction apparatus and heated to 250° C. in flowing hydrogen. The flow was maintained at temperature for 2 hours at 250° C. after which the apparatus and catalyst was cooled.
  • the dried catalyst contained 0.15% by weight Pt and 0.022% by weight Mn.
  • Example 3 was repeated with the exception that the second solution was made using cobalt nitrate (Co(NO 3 ) 2 ⁇ 6H 2 O) instead of manganese nitrate and contained 1% of Co by weight.
  • the dried catalyst contained 0.15% by weight Pt and 0.023% by weight Co.
  • Example 4 was repeated using as a first solution a solution of palladium nitrate (Pd(NO 3 ) 4 ) made as described in Example 1.
  • the resulting catalyst contained 0.15% by weight Pd and 0.023% by weight Co.
  • Example 1 The method of Example 1 was repeated using a single solution of 2 g of platinum nitrate (Pt(NO 3 ) 4 ) made up to 60 ml in demineralised water.
  • the resulting catalyst contained 0.15% by weight Pt.
  • Example 1 The method of Example 1 was repeated using a single solution of palladium nitrate (Pd(NO 3 ) 2 ) made up to 60 ml in demineralised water.
  • the resulting catalyst contained 0.15% by weight Pd.
  • the catalysts were tested as whole spheres in a 1′′ (2.54 mm) diameter tubular stainless steel reactor equipped with a thermocouple for measuring catalyst bed temperature.
  • the bulk volume of catalyst charged for each test run was 15 ml and the catalyst charge was located between two beds of inert alumina particles with each layer being separated by a small plug of glass wool.
  • the reactor was connected to a test rig and pressure tested to approximately 2.5 bar-g.
  • a flow of gas of composition 0.1% O 2 in nitrogen was established to the reactor via independent mass flow controllers at a GHSV of 15000 h ⁇ 1 (flow rate ⁇ 3.8 litres/min).
  • the gas pre-heater and reactor were heated to 300-320° C. over approx. 1 hour.
  • a liquid flow of ethylene glycol was then established to the pre-heater where it was vaporised and mixed with the 0.1% O 2 in nitrogen feed prior to being fed to the reactor.
  • the process gas composition as it entered the reactor was 1000 ppm oxygen, 400 ppm ethylene glycol with the balance being nitrogen.
  • the oxygen content of the gas stream was measured using an OrbisphereTM on-line oxygen analyser. Gas compositions are given by volume.
  • the system was allowed to equilibrate at each temperature for 0.5-1 hour before the oxygen measurement was taken. Percent (%) conversion versus temperature is shown plotted for each catalyst tested in FIG. 1 .
  • the mixed solution was added slowly to the tumbling pellets in aliquots over about 10 minutes.
  • the tumbling was continued for a further 15 minutes, and then the catalyst was dried overnight in air at 105° C.
  • the dried catalyst was then transferred to a reduction apparatus and heated to 250° C. in flowing hydrogen. The flow was maintained for 2 hours at 250° C. after which the apparatus and catalyst was cooled.
  • the dry catalyst contained 0.15% Pt, 0.08% Ru and 5% Ce.
  • the mixed solution containing the three metal salts was then diluted to a final volume of 143 ml with demineralised water to form the co-impregnation solution.
  • 198 g of alumina support were charged to a laboratory tumbling apparatus and tumbled slowly at about 2 rpm.
  • the mixed impregnation solution was added slowly to the tumbling pellets in aliquots over about 10 minutes.
  • the tumbling was continued for a further 15 minutes, and then the catalyst was dried overnight in an air oven at 105° C.
  • the dried Ce-promoted catalyst was then transferred to a reduction apparatus and heated to 250° C. in flowing hydrogen over 1.5 hours. The flow was maintained for 2 hours at 250° C. after which the apparatus and catalyst was cooled.
  • the dry catalyst contained 0.15% Pt, 0.08% Ru and 5% Ce.
  • Example 9 40 mg of crushed catalyst made in Example 9 was tested for use in the oxidation of ethylene glycol at 190° C.
  • the gas feed stream composition was 400 ppm ethylene glycol and 700 ppm oxygen in nitrogen. In this system, 1000 ppm oxygen is required for complete stoichiometric reaction to carbon dioxide and water and so the conditions were sub-stoichiometric on oxygen.
  • the results are plotted in FIG. 2 together with results obtained from a catalyst containing 0.15% Pt, 0.08% Ru and no Ce. The results show that the cerium-promoted catalyst retains significantly higher conversion than the un-promoted catalyst over the duration of the test.
  • the dried catalyst was transferred to a reduction apparatus and heated to 320° C. in a flow of 5% hydrogen in nitrogen. The flow was maintained at this temperature for 2 hours, after which the apparatus and catalyst were allowed to cool.
  • the dry catalyst contained 0.15% Pt and 0.08% Ru.

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US13/119,605 2008-09-18 2009-09-17 Catalyst and process Active 2031-08-31 US8945497B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB0817109.2A GB0817109D0 (en) 2008-09-18 2008-09-18 Catalyst and process
GB0817109.2 2008-09-18
PCT/GB2009/051208 WO2010032051A1 (fr) 2008-09-18 2009-09-17 Catalyseur et procédé

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US20150014592A1 (en) * 2013-07-11 2015-01-15 Sabic Global Technologies B.V. Use of lanthanide oxides to reduce sintering of catalysts
US20220072513A1 (en) * 2018-12-21 2022-03-10 Hanwha Solutions Corporation Method for manufacturing ruthenium oxide-supported catalyst for preparing chlorine and catalyst manufactured thereby
US20220080395A1 (en) * 2018-12-21 2022-03-17 Hanwha Solutions Corporation Hydrogen chloride oxidation reaction catalyst for preparing chlorine, and preparation method terefor

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US9415374B2 (en) * 2012-04-18 2016-08-16 Dsm Ip Assets B.V. Device useful for hydrogenation reactions (III)
CN105056970B (zh) * 2015-08-17 2018-12-11 中自环保科技股份有限公司 一种柴油车催化剂型颗粒物净化器的制备方法
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US20150014592A1 (en) * 2013-07-11 2015-01-15 Sabic Global Technologies B.V. Use of lanthanide oxides to reduce sintering of catalysts
US9314771B2 (en) * 2013-07-11 2016-04-19 Sabic Global Technologies B.V. Use of lanthanide oxides to reduce sintering of catalysts
US9731273B2 (en) 2013-07-11 2017-08-15 Sabic Global Technologies B.V. Use of lanthanide oxides to reduce sintering of catalysts
US20220072513A1 (en) * 2018-12-21 2022-03-10 Hanwha Solutions Corporation Method for manufacturing ruthenium oxide-supported catalyst for preparing chlorine and catalyst manufactured thereby
US20220080395A1 (en) * 2018-12-21 2022-03-17 Hanwha Solutions Corporation Hydrogen chloride oxidation reaction catalyst for preparing chlorine, and preparation method terefor

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TWI498159B (zh) 2015-09-01
CN102176957B (zh) 2014-06-25
KR20110053481A (ko) 2011-05-23
EP2326407A1 (fr) 2011-06-01
EA201170460A1 (ru) 2011-10-31
EA025109B1 (ru) 2016-11-30
CN102176957A (zh) 2011-09-07
TW201026385A (en) 2010-07-16
WO2010032051A1 (fr) 2010-03-25
US20110229396A1 (en) 2011-09-22
MX2011003008A (es) 2011-06-27
EP2326407B1 (fr) 2020-03-04

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